Please use this identifier to cite or link to this item:
https://hdl.handle.net/11499/7438
Title: | Zinc oxide nanoparticles: Genotoxicity, interactions with UV-light and cell-transforming potential | Authors: | Demir, E. Akça, Hakan Kaya, B. Burgucu, D. Tokgün, O. Turna, F. Aksakal, S. |
Keywords: | Comet assay Genotoxicity Micronucleus assay Soft-agar assay UV-light interaction ZnO nanoparticles Algae Anchorages (foundations) Cell growth Cells Cytology Enzymes Nanoparticles Polysaccharides Tissue culture Cell transformation Comet assays Genotoxicities Human embryonic kidneys Mouse embryonic fibroblasts UV-light Zinc oxide nanoparticles Zinc oxide agar DNA formamidopyrimidine glycosylase endonuclease endonuclease iii nanoparticle unclassified drug zinc oxide bioassay database genotoxicity nanotechnology public health rodent ultraviolet radiation zinc animal cell article cell anchorage cell growth cell strain 3T3 cell strain HEK293 cell transformation comet assay controlled study DNA damage embryo fibroblast human human cell in vitro study micronucleus micronucleus test mouse nonhuman ultraviolet B radiation Animals Cell Transformation, Neoplastic Comet Assay HEK293 Cells Humans Mice Micronucleus Tests NIH 3T3 Cells Ultraviolet Rays Zinc Oxide |
Publisher: | Elsevier | Abstract: | The in vitro genotoxic and the soft agar anchorage independent cell transformation ability of zinc oxide nanoparticles (NPs) and its bulky forms have been evaluated in human embryonic kidney (HEK293) and in mouse embryonic fibroblast (NIH/3T3) cells, either alone or in combination with UVB-light. The comet assay, with and without the use of FPG and Endo III enzymes, the micronucleus assay and the soft-agar colony assay were used. For the comet assay a statistically significant induction of DNA damage, with and without the enzymes, were observed up of 100. µg/mL. ZnO NPs were able to increase significantly the frequency of micronuclei, and similar results were observed in the cell transformation assay where such NPs were able to induce cell-anchorage independent growth. These effects were observed at doses up 100. µg/mL. Although UVB-light was able to induce genotoxic damage and cell-anchorage growth, a significant antagonist interaction effect was observed in combination with ZnO NPs. These in vitro results, obtained with the selected cell lines, contribute to increase our genotoxicity database on the ZnO NPs effects as well as to open the discussion about their risk in photo-protection sun screens. © 2013 Elsevier B.V. | URI: | https://hdl.handle.net/11499/7438 https://doi.org/10.1016/j.jhazmat.2013.11.043 |
ISSN: | 0304-3894 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
Show full item record
CORE Recommender
SCOPUSTM
Citations
64
checked on Nov 16, 2024
WEB OF SCIENCETM
Citations
64
checked on Nov 16, 2024
Page view(s)
42
checked on Aug 24, 2024
Google ScholarTM
Check
Altmetric
Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.